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http://dx.doi.org/10.5141/JEFB.2010.33.3.223

Controlling environmental factors of soil enzyme activities at three altitudes on Mt. Jumbong  

Jang, In-Young (School of Civil and Environmental Engineering, Yonsei University)
Kang, Ho-Jeong (School of Civil and Environmental Engineering, Yonsei University)
Publication Information
Journal of Ecology and Environment / v.33, no.3, 2010 , pp. 223-228 More about this Journal
Abstract
Soil microbes perform crucial roles in the nutrient cycles of forest ecosystems, by effecting the decomposition of organic matter. Enzyme activities have been used to evaluate decomposition rates, as well as microbial activities. The principal objectives of this study were to determine the activities of different soil enzymes, to compare enzyme activities at different elevations, and to elucidate the most important controlling variables for enzyme activities. We conducted a field survey at three sites in Mt. Jumbong on a monthly basis from May, 2004 to September, 2005. Enzyme activities did not change substantially over different seasons. However, the spatial differences were distinct; the lowest elevation site evidenced the lowest levels of enzyme activity. Soils at the lowest elevation were nutrient-depleted soils, and enzyme activities appeared to be affected by precipitation and temperature. However, enzyme activities in fertile soils at high elevations were associated with nutrients and organic matter. The enzyme activities detected in this study differed significantly at the three elevations, and their controlling variables also evidenced different factors.
Keywords
controlling factors; enzyme activities; forest soil; spatial variations;
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1 Sinsabaugh RL, Hill BH, Shah JJF. 2009. Ecoenzymatic stoichiometry of microbial organic nutrient acquisition in soil and sediment. Nature 462: 795-798.   DOI
2 Speir TW, Cowling JC. 1991. Phosphatase activities of pasture plants and soils: relationship with plant productivity and soil P fertility indices. Biol Fertil Soils 12: 189-194.   DOI
3 Killham K, Staddon WJ. 2002. Bioindicators and sensors of soil health and the application of geostatistics. In: Enzymes in the Environment: Activity, Ecology, and Applications (Burns RG, Dick RP, eds). Marcel Dekker, New York, NY, pp 391-405.
4 Kourtev PS, Ehrenfeld JG, Haggblom M. 2002. Exotic plant species alter the microbial community structure and function in the soil. Ecology 83: 3152-3166.   DOI
5 Orchard VA, Cook FJ. 1983. Relationship between soil respiration and soil moisture. Soil Biol Biochem 15: 447-453.   DOI
6 Paul EA, Clark FE. 1989. Soil Microbiology and Biochemistry. Academic Press, New York, NY.
7 Kang H, Lee D. 1998. Changes of soil enzyme activities by simulated acid and nitrogen deposition. Chem Ecol 14: 123-131.   DOI
8 Keeney DR, Nelson DW. 1982. Indophenol-blue method. In: Methods of Soil Analysis: Part. 2. Chemical and Microbiologial Properties (Page AL, Milier RH, Keeney DR, eds). 2nd ed. American Society of Agronomy, Madison, WI, pp 674-676.
9 Kennedy AC, Gewin VL. 1997. Soil microbial diversity: present and future considerations. Soil Sci 162: 607-617.   DOI
10 Kang SY, Doh S, Lee D, Lee D, Jin VL, Kimball JS. 2003. Topographic and climatic controls on soil respiration in six temperate mixed-hardwood forest slopes, Korea. Global Change Biol 9: 1427-1437.   DOI
11 Halvorson JJ, Smith JL, Papendick RI. 1996. Integration of multiple soil parameters to evaluate soil quality: a field example. Biol Fertil Soils 21: 207-214.   DOI
12 Kang H, Freeman C. 1999. Phosphatase and arylsulphatase activities in wetland soils: annual variation and controlling factors. Soil Biol Biochem 31: 449-454.   DOI
13 Kang H, Freeman C. 2009. Soil enzyme analysis for leaf litter decomposition in global wetlands. Commun Soil Sci Plan Anal 40: 3323-3334.   DOI
14 Hopkins DW, Sparrow AD, Elberling B, Gergorich EG, Novis PM, Greenfield LG, Tilston EL. 2006. Carbon, nitrogen and temperature controls on microbial activity in soils from an Antarctic dry valley. Soil Biol Biochem 38: 3130-3140.   DOI
15 Jia B, Zhou G, Wang Y, Wang F, Wang X. 2006. Effects of temperature and soil water-content on soil respiration of grazed and ungrazed Leymus chinensis steppes, Inner Mongolia. J Arid Environ 67: 60-76.   DOI
16 Jin X, Wang S, Zhou Y. 2008. Microbial $CO_2$ production from surface and subsurface soil as affected by temperature, moisture, and nitrogen fertilisation. Aust J Soil Res 46: 273-280.   DOI
17 Jordan D, Ponder F Jr, Hubbard VC. 2003. Effects of soil compaction, forest leaf litter and nitrogen fertilizer on two oak species and microbial activity. Appl Soil Ecol 23: 33-41.   DOI
18 Enowashu E, Poll C, Lamersdorf N, Kandeler E. 2009. Microbial biomass and enzyme activities under reduced nitrogen deposition in a spruce forest soil. Appl Soil Ecol 43: 11-21.   DOI
19 Harrison AF. 1983. Relationship between intensity of phosphatase activity and physico-chemical properties in woodland soils. Soil Biol Biochem 15: 93-99.   DOI
20 Haussling M, Marschner H. 1989. Organic and inorganic soil phosphates and acid phosphatase activity in the rhizosphere of 80-year-old Norway spruce (Picea abies (L.) Karst.) trees. Biol Fertil Soils 8: 128-133.
21 Anderson JM, Ingram JSI. 1993. Tropical Soil Biology and Fertility: A Handbook of Methods. 2nd ed. C.A.B. International, Wallingford, pp 74-75.
22 Andersson S, Nilsson SI. 2001. Influence of pH and temperature on microbial activity, substrate availability of soil-solution bacteria and leaching of dissolved organic carbon in a mor humus. Soil Biol Biochem 33: 1181-1191.   DOI
23 Waring RH, Schlesinger WH. 1986. Forest Ecosystems: Concepts and Management. Academic Press, New York, NY.
24 Boerner REJ, Brinkman JA, Smith A. 2005. Seasonal variations in enzyme activity and organic carbon in soil of a burned and unburned hardwood forest. Soil Biol Biochem 37: 1419-1426.   DOI
25 Bonnett SAF, Ostle N, Freeman C. 2006. Seasonal variations in decomposition processes in a valley-bottom riparian peatland. Sci Total Environ 370: 561-573.   DOI
26 Acosta-Martinez V, Cruz L, Sotomayor-Ramirez D, Perez-Alegria L. 2007. Enzyme activities as affected by soil properties and land use in a tropical watershed. Appl Soil Ecol 35: 35-45.   DOI
27 Wright AL, Reddy KR. 2001. Phosphorus loading effects on extracellular enzyme activities in Everglades Wetland Soils. Soil Sci Soc Am J 65: 588-595.   DOI
28 Ye R, Wright AL, Inglett K, Wang Y, Ogram AV, Reddy KR. 2009. Land-use effects on soil nutrient cycling and microbial community dynamics in the Everglades Agricultural Area, Florida. Commun Soil Sci Plant Anal 40: 2725-2742.   DOI
29 Allison SD, Czimczik CI, Treseder KK. 2008. Microbial activity and soil respiration under nitrogen addition in Alaskan boreal forest. Global Change Biol 14: 1156-1168.   DOI
30 Zak JC, Willig MR, Moorhead DL, Wildman HG. 1994. Functional diversity of microbial communities: a quantitative approach. Soil Biol Biochem 26: 1101-1108.   DOI
31 Wellington EMH, Berry A, Krsek M. 2003. Resolving functional diversity in relation to microbial community structure in soil: exploiting genomics and stable isotope probing. Curr Opin Microbiol 6: 295-301.   DOI
32 Stark JM, Firestone MK. 1995. Mechanisms for soil moisture effects on activity of nitrifying bacteria. Appl Environ Microbiol 61: 218-221.
33 Winkler JP, Cherry RS, Schlesinger WH. 1996. The $Q_{10}$ relationship of microbial respiration in a temperate forest soil. Soil Biol Biochem 28: 1067-1072.   DOI
34 Ushio M, Kitayama K, Balser TC. Tree species effects on soil enzyme activities through effects on soil physicochemical and microbial properties in a tropical montane forest on Mt. Kinabalu, Borneo. Pedobiology. (in press)
35 Vance ED, Chapin FS. 2001. Substrate limitations to microbial activity in taiga forest floors. Soil Biol Biochem 33: 173-188.   DOI
36 Waldrop MP, Balser TC, Firestone MK. 2000. Linking microbial community composition to function in a tropical soil. Soil Biol Biochem 32: 1837-1846.   DOI
37 Speir TW, Ross DJ. 2002. Hydrolytic enzyme activities to assess soil degradation and recovery. In: Enzymes in the Environment: Activity, Ecology, and Applications (Burns RG, Dick RP, eds). Marcel Dekker, New York, NY, pp 407-432.
38 Trasar-Cepeda C, Leiros MC, Gil-Sotres F. 2000. Biochemical properties of acid soils under climax vegetation (Atlantic oakwood) in an area of the European temperate-humid zone (Galicia N.W. Spain): specific parameters. Soil Biol Biochem 32: 747-755.   DOI